A 101 to Qualified Person (QP) Release in Clinical Trial Supply

Understanding pharmaceutical legislation is vital for successfully navigating the complex global clinical trials market and ensuring the timely supply of your Investigational Medicinal Products (IMPs). In Europe the Qualified Person (QP) plays a crucial role in bringing safe and timely products to the market. For pharmaceutical companies based outside of Europe it is important to understand European GMP requirements and the role and responsibilities of the QP. In this Pharma IQ 101 we highlight... To continue reading this story Click Here